The effect of miRNA and autophagy on colorectal cancer.
The effect of miRNA and autophagy on colorectal cancer.
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DOI:
10.1111/cpr.12900
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发表时间:
2020-10
影响因子:
8.5
通讯作者:
Zhu W
中科院分区:
文献类型:
--
作者:
Long J;He Q;Yin Y;Lei X;Li Z;Zhu W
Colorectal cancer (CRC) has become a concern because of its high recurrence rate and metastasis rate, low early diagnosis rate and poor therapeutic effect. At present, various studies have shown that autophagy is closely connected with the occurrence and progression of CRC. Autophagy is a highly cytosolic catabolic process involved in lysosomes in biological evolution. Cells degrade proteins and damaged organelles by autophagy to achieve material circulation and maintain cell homeostasis. Moreover, microRNAs are key regulators of autophagy, and their mediated regulation of transcriptional and post‐transcriptional levels plays an important role in autophagy in CRC cells. This review focuses on the recent research advances of how autophagy and related microRNAs are involved in affecting occurrence and progression of CRC and provides a new perspective for the study of CRC treatment strategies. Regulatory relationship between miRNAs and autophagy in CRC. Autophagy consists of a series of activities, such as phagophore formation, elongation, autophagosome and fusion with lysosome to form autolysosome. MiRNAs exert dual regulatory effects on autophagy pathways related to CRC through indirect or direct pathways. In the figure, the purple box represents autophagy‐related proteins, which indirectly regulate the autophagy process (eg, Bcl‐2, mTOR), the green box represents autophagy‐associated proteins, which are directly involved in the occurrence or formation of autophagy (eg, Beclin 1, LC3), and the yellow box represents the cellular process.
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影响因子:
4.6
作者:
Che, Jing;Wang, Wenshan;Yuan, Xianglin
通讯作者:
Yuan, Xianglin
DOI:
10.1158/1078-0432.ccr-09-1249
发表时间:
2009-12-01
期刊:
Clinical cancer research : an official journal of the American Association for Cancer Research
影响因子:
--
作者:
Gulhati P;Cai Q;Li J;Liu J;Rychahou PG;Qiu S;Lee EY;Silva SR;Bowen KA;Gao T;Evers BM
通讯作者:
Evers BM
影响因子:
3.4
作者:
Adekola K;Rosen ST;Shanmugam M
通讯作者:
Shanmugam M
影响因子:
45.3
作者:
Bécouarn, Y;Ychou, M;Rougier, P
通讯作者:
Rougier, P
影响因子:
50.3
作者:
Calon A;Espinet E;Palomo-Ponce S;Tauriello DV;Iglesias M;Céspedes MV;Sevillano M;Nadal C;Jung P;Zhang XH;Byrom D;Riera A;Rossell D;Mangues R;Massagué J;Sancho E;Batlle E
通讯作者:
Batlle E